"72205-239-64" National Drug Code (NDC)

NDC Code	72205-239-64
Package Description	4 BLISTER PACK in 1 CARTON (72205-239-64) / 28 CAPSULE in 1 BLISTER PACK
Product NDC	72205-239
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nilotinib
Non-Proprietary Name	Nilotinib
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20251119
Marketing Category Name	ANDA
Application Number	ANDA218544
Manufacturer	Novadoz Pharmaceuticals LLC
Substance Name	NILOTINIB
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA], UGT1A1 Inhibitors [MoA]